Trigowiin A

Details

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Internal ID 234bef6b-c61c-479f-914b-47141948fd40
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Tigliane and ingenane diterpenoids > Phorbol esters
IUPAC Name [(1S,2S,6R,10S,11R,13S,14R,15R)-13-acetyloxy-1,6-dihydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5,9-dioxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,7-dienyl] dodecanoate
SMILES (Canonical) CCCCCCCCCCCC(=O)OC1C(C2(C3C=C(C(=O)C3(C=C(C(=O)C2C4C1(C4(C)C)OC(=O)C)CO)O)C)O)C
SMILES (Isomeric) CCCCCCCCCCCC(=O)O[C@@H]1[C@H]([C@@]2([C@@H]3C=C(C(=O)[C@]3(C=C(C(=O)[C@H]2[C@H]4[C@@]1(C4(C)C)OC(=O)C)CO)O)C)O)C
InChI InChI=1S/C34H50O9/c1-7-8-9-10-11-12-13-14-15-16-25(37)42-30-21(3)33(41)24-17-20(2)29(39)32(24,40)18-23(19-35)27(38)26(33)28-31(5,6)34(28,30)43-22(4)36/h17-18,21,24,26,28,30,35,40-41H,7-16,19H2,1-6H3/t21-,24-,26+,28-,30-,32-,33+,34-/m1/s1
InChI Key KWBZHXARNUSVGU-SNDKCSAGSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C34H50O9
Molecular Weight 602.80 g/mol
Exact Mass 602.34548317 g/mol
Topological Polar Surface Area (TPSA) 147.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 9
H-Bond Donor 3
Rotatable Bonds 13

Synonyms

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CHEMBL2208234

2D Structure

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2D Structure of Trigowiin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9682 96.82%
Caco-2 - 0.7977 79.77%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7797 77.97%
OATP2B1 inhibitior - 0.8605 86.05%
OATP1B1 inhibitior + 0.8212 82.12%
OATP1B3 inhibitior + 0.9293 92.93%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.5593 55.93%
BSEP inhibitior + 0.8201 82.01%
P-glycoprotein inhibitior + 0.7639 76.39%
P-glycoprotein substrate + 0.6446 64.46%
CYP3A4 substrate + 0.6809 68.09%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9180 91.80%
CYP3A4 inhibition - 0.7834 78.34%
CYP2C9 inhibition + 0.7435 74.35%
CYP2C19 inhibition - 0.8886 88.86%
CYP2D6 inhibition - 0.9083 90.83%
CYP1A2 inhibition - 0.8407 84.07%
CYP2C8 inhibition + 0.6659 66.59%
CYP inhibitory promiscuity - 0.7544 75.44%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6715 67.15%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9139 91.39%
Skin irritation - 0.5114 51.14%
Skin corrosion - 0.9549 95.49%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3769 37.69%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8511 85.11%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.5888 58.88%
Acute Oral Toxicity (c) III 0.5840 58.40%
Estrogen receptor binding + 0.7213 72.13%
Androgen receptor binding + 0.7255 72.55%
Thyroid receptor binding - 0.5297 52.97%
Glucocorticoid receptor binding + 0.6746 67.46%
Aromatase binding + 0.6779 67.79%
PPAR gamma + 0.5786 57.86%
Honey bee toxicity - 0.8102 81.02%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.7429 74.29%
Fish aquatic toxicity + 0.9917 99.17%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2996 Q05655 Protein kinase C delta 98.50% 97.79%
CHEMBL2581 P07339 Cathepsin D 97.52% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.33% 96.09%
CHEMBL299 P17252 Protein kinase C alpha 96.99% 98.03%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.99% 91.11%
CHEMBL3045 P05771 Protein kinase C beta 92.95% 97.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.28% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.53% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.44% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.27% 99.17%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 86.33% 91.24%
CHEMBL1937 Q92769 Histone deacetylase 2 85.67% 94.75%
CHEMBL5255 O00206 Toll-like receptor 4 84.71% 92.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.93% 99.23%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.16% 92.86%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.94% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.34% 82.69%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.07% 97.29%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.92% 95.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.51% 90.08%
CHEMBL1907 P15144 Aminopeptidase N 80.44% 93.31%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Trigonostemon howii

Cross-Links

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PubChem 71456088
NPASS NPC19464
ChEMBL CHEMBL2208234